Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Evrim Kargın Çakıcı"'
Autor:
Esra Bağlan, Semanur Özdel, Tülin Güngör, Deniz Karakaya, Evra Çelikkaya, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Mehmet Bülbül
Publikováno v:
The Journal of Pediatric Academy, Vol 2, Iss 3, Pp 101-105 (2021)
ABSTRACT Objectives: Behçet’s disease (BD) is a multisystemic inflammatory disease with unknown etiology. It is characterized by recurrent oral and genital ulcerations, uveitis, and skin lesions, various musculoskeletal, gastrointestinal, centr
Externí odkaz:
https://doaj.org/article/413ae57251fc4e85873abea5dd28a061
Autor:
Fatma Yazılıtaş, Semanur Özdel, Doğan Şimşek, Özlem Aydoğ, Evrim Kargın Çakıcı, Gökçe Gür Can, Tülin Güngör, Mehmet Bülbül
Publikováno v:
São Paulo Medical Journal, Vol 137, Iss 6, Pp 517-522 (2020)
ABSTRACT BACKGROUND: Juvenile idiopathic arthritis (JIA) is the commonest chronic rheumatic disease among children. When not treated effectively, JIA can lead to functional disability, due to joint damage, along with long-term morbidities. OBJECTIVES
Externí odkaz:
https://doaj.org/article/e0fc2c7979a643e3ab324b4a143e5ec3
Autor:
Fatma Yazılıtaş, Evrim Kargın Çakıcı, Ayse Secil Eksioglu, Tülin Güngör, Evra Çelikkaya, Deniz Karakaya, Çiğdem Üner, Mehmet Bülbül
Publikováno v:
Hospital Practice. 51:82-88
Autor:
Deniz Karakaya, Tülin Güngör, Evrim Kargın Çakıcı, Fatma Yazılıtaş, Evra Çelikkaya, Mehmet Bülbül
Background Nephrotic syndrome is the most common glomerular disorder of childhood and data on complications are still limited and predisposing risk factors have not been fully defined. The aim of our study is to systematically evaluate treatment and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5eb2a01b5581877e830e66a7c054bc29
https://doi.org/10.21203/rs.3.rs-2864783/v1
https://doi.org/10.21203/rs.3.rs-2864783/v1
Autor:
Evra, Çelikkaya, Tülin, Güngör, Deniz, Karakaya, Evrim, Kargın Çakıcı, Fatma, Yazılıtaş, Fatih, Özaltın, Mehmet, Bülbül
Publikováno v:
Experimental and Clinical Transplantation. 20:45-48
Membranoproliferative glomerulonephritis and renal microangiopathies may manifest similar clinical presentations and histology. Many genetic mutations that cause these diseases have been reported. Studies on mutations in the gene encoding diacylglyce
Autor:
Esra Bağlan, Deniz Karakaya, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Mehmet Bülbül, Semanur Özdel, Tülin Güngör, Evra Çelikkaya
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e413-e417
Henoch-Schonlein purpura (HSP) is the most common childhood systemic vasculitis. The present study aims to investigate the effectiveness of the immature granulocyte (IG) percentage as a new marker for predicting internal organ involvement in HSP. Thi
Autor:
Mehmet Bülbül, Semanur Özdel, Esra Bağlan, Evrim Kargın Çakıcı, Saliha Senel, Husniye Yucel, Fatma Yazılıtaş
Publikováno v:
Pediatrics International. 63:636-642
Background Juvenile idiopathic arthritis (JIA) is the most common chronic rheumatologic disease of childhood. The various subtypes of JIA differ in clinical features and treatments. The aim of this study was to analyze the frequency of JIA subtypes,
Autor:
Fatma Yazılıtaş, Evrim Kargın Çakıcı, Eda Didem Kurt Şükür, Semanur Özdel, Tülin Güngör, Esra Bağlan, Evra Çelikkaya, Deniz Karakaya, Diclehan Orhan, Mehmet Bülbül
Publikováno v:
Postgraduate medicine. 134(4)
Immunoglobulin A (IgA) vasculitis (also known as Henoch-Schonlein purpura) is the most common small vessel vasculitis of childhood. The long-term prognosis depends on renal involvement. The aim of this study was to evaluate the risk factors associate
Autor:
Michael Ludwig, Fatma Yazılıtaş, Evrim Kargın Çakıcı, Gökçe Gür, Fehime Kara Eroglu, Mehmet Bülbül, Tülin Güngör
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
Dent disease is a rare X-linked recessive tubular disorder, characterized by the triad of low molecular-weight proteinuria, hypercalciuria, nephrocalcinosis and/or nephrolithiasis. It is caused by mutations in the CLCN5 gene or OCRL gene. Thirty to 8
Autor:
Esra Bağlan, Semanur Özdel, Tülin Güngör, Evra Çelikkaya, Mehmet Bülbül, Gökçe Gür, Fatma Yazılıtaş, Evrim Kargın Çakıcı
Publikováno v:
Acta Clinica Belgica. 76:294-299
Objective: Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by recurrent, self-limited attacks of fever with serositis. Acute recurrent arthritis is the most commo...